Canonical Allele Identifier: PA658673970
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482539
ClinVar RCV Id: RCV000562139 RCV001835854
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly724Asp
CA382538803
NM_000051.4:c.2171G>A